HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 919169Generated: October 31, 2026
Trifluoromethylsulfinylchloride → 5-amino-1-(2-chloro-6-fluoro-4-(trifluoromethyl)phenyl)-4-(trifluoromethylsulfinyl)-1H-pyrazole-3-carbonitrile
https://huagongshe.com/reaction/919169
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoromethylsulfinylchloride | HCID 11008121 | — |
| Reactant | Dimethylamine p-toluenesulfonate | HCID 12199009 | — |
| Reactant | 5-amino-1-(2-chloro-6-fluoro-4-(trifluoromethyl)-phenyl)-1H-pyrazole-3-carbonitrile | HCID 68409371 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-amino-1-(2-chloro-6-fluoro-4-(trifluoromethyl)phenyl)-4-(trifluoromethylsulfinyl)-1H-pyrazole-3-carbonitrile | HCID 89858790 | 64.6% |
Reaction Steps
To a solution of 5-amino-1-(2-chloro-6-fluoro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile (140 g, 459.6 mmol, 1.00 eq.) and dimethylamine tosylate (151.8 g, 698.6 mmol, 1.52 eq.) in toluene (840 mL) was added CF3SOCl (89.7 g, 588.3 mmol, 1.28 eq.). After the mixture was stirred at 40° C. for 16 h, nitrogen was bubbled through the solution and the solution was cooled to rt. Then the mixture was poured into 2 L ice/water and stirred at 0° C. for 1 h. The precipitated solid was isolated by filtration and dried under vacuum. The solid was recrystallized with toluene to give 5-amino-1-(2-chloro-6-fluoro-4-(trifluoromethyl)phenyl)-4-(trifluoromethylsulfinyl)-1H-pyrazole-3-carbonitrile (125 g, 64%) as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273007B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-9dac93fa030f492ba721f2b855d99919 |
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| Source note | uspto-grants-2016_03 |
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